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A new family of aphids (Hemiptera, Sternorrhyncha) from the Lower Cretaceous of Baissa, Transbaikalia

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A new family of aphids (Hemiptera, Sternorrhyncha)

from the Lower Cretaceous of Baissa, Transbaikalia

Agnieszka Homan†, Piotr Wegierek

Department of Zoology, University of Silesia, Bankowa 9, 40-007 Katowice, Poland

urn:lsid:zoobank.org:author:4C880EDB-ABCE-49FF-81C6-B9F82CABBDAA urn:lsid:zoobank.org:author:5DEB5123-5E2E-4FF2-BFBA-0D974720252B

Corresponding author: Agnieszka Homan (agnieszka.homan@rappid.pl)

Academic editor: D. Shcherbakov  |  Received 28 April 2011  |  Accepted 13 July 2011  |  Published 27 September 2011 urn:lsid:zoobank.org:pub:7A75FC18-C9F2-4A15-8D4A-BCED31172FC6

Citation: Homan A, Wegierek P (2011) A new family of aphids (Hemiptera, Sternorrhyncha) from the Lower Cretaceous of Baissa, Transbaikalia. In: Shcherbakov DE, Engel MS, Sharkey MJ (Eds) Advances in the Systematics of Fossil and Modern Insects: Honouring Alexandr Rasnitsyn. ZooKeys 130: 167–174. doi: 10.3897/zookeys.130.1444

Abstract

The family Rasnitsynaphididae fam. n. has a unique combination of characters: 9-segmented antennae; rhinaria arranged in many transverse rows, surrounding the antennal segments; segment IX narrower than other segments of flagellum, always without rhinaria; cubitus branches separated; ovipositor present; siphuncular pores absent. The new family comprises the genus Rasnitsynaphis gen. n. with three species,

R. ennearticulata sp. n., R. coniuncta sp. n., and R. quadrata sp. n., all from the Lower Cretaceous of Transbaikalia.

Keywords

Hemiptera, aphids, fossil insects, Lower Cretaceous, Baissa, new family, new genus, new species

Introduction

Baissa is one of the most important Lower Cretaceous insect fossil sites. The outcrop is located in the Asian part of Russia, in western Transbaikalia, on the left bank of the Vitim River. The exact age of lacustrine sediments of the Zaza Formation at Baissa is

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disputable, usually estimated as Early Cretaceous (Neocomian–Aptian), however most paleoentomologists date them as Valanginian–Hauterivian (Zherikhin et al. 1999).

More than 20 000 fossil insects (including above 2 500 aphid specimens), often of excellent preservation state, have been collected there. Nearly all aphids from Baissa belong to three families: Ellinaphididae Kania & Wegierek, 2008, Szelegiewicziidae Wegierek, 1989 (both in Palaeoaphidoidea), and Oviparosiphidae Shaposhnikov, 1979 (Aphidoidea). The new taxa described below show an even higher morphological diver-sity of aphids in the Lower Cretaceous.

Material and methods

The material comes from the collection of the Laboratory of Arthropods, Paleonto-logical Institute (PIN), Russian Academy of Sciences, Moscow, where it is currently stored. The research methods did not differ substantially from those widely used in paleoentomological research (Rasnitsyn 2002). The imprints were photographed under the stereoscopic and the light microscope. The graphics tablet was applied to make the drawings on the photographic layer in Adobe Photoshop. In case when the specimen was represented by two imprints, the drawings are based on both re-verse and obre-verse, while the photograph presents only one imprint. The number of rhinaria given in the descriptions always relates only to the one side of the antenna. It results from the lack or the weak preservation of one of the imprints. All measure-ments are given in mm.

Taxonomy

Hemiptera Linnaeus, 1758

Sternorrhyncha Amyot & Serville, 1843

Aphidomorpha Becker-Migdisova & Aizenberg, 1962

Rasnitsynaphididae fam. n.

urn:lsid:zoobank.org:act:94C0708C-7F79-426A-B9FB-1DD3D53BAF67 http://species-id.net/wiki/Rasnitsynaphididae

Type genus.Rasnitsynaphis gen. n.

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Rasnitsynaphisgen. n.

urn:lsid:zoobank.org:act:2466FD65-63B1-4F19-9BC1-576C84461B21 http://species-id.net/wiki/Rasnitsynaphis

Type species.Rasnitsynaphis ennearticulata sp. n.

Etymology. Named to honour Alexandr P. Rasnitsyn, who is not only eminent researcher, but also a teacher of many paleoentomologists. P.W. is honoured to be one of his students.

Diagnosis. As for family.

Description. Body massive. Front edge of head convex. Head with epicranial su-ture. Rostrum shorter than body, reaching to the middle of abdomen. Antennae longer than one third of the body length but shorter than its half. Antennal segment III 2–4 times as long as wide; segments IV-VIII of the same length or nearly so. Surface of all segments of flagellum sculptured in form of transverse ribs. Rhinaria ellipsoidal, ar-ranged in more or less dense rows which are sometimes joined. Cubital vein CuA1 2.5 times longer than CuA2. Pterostigma big, spindle-shaped, pointed, 3–3.5 times as long as wide. Vein Rs slightly bent at base. Media with two or three branches. Bifurcation of vein M into M1 and M2 or into M1+2 and M3 just beyond the base of vein Rs.

Key to species of Rasnitsynaphis

1 Antennae short, about 1/2 of thorax height, segment III two times as long as wide, with ca. 9 rows of rhinaria; segments IV–VIII as long as wide; M with 2 branches ...R. quadrata sp. n.

– Antennae longer, segment III three to four times as long as wide; segments IV–VIII longer than wide ...2

2 Segment III four times as long as wide, with ca. 11 rows of rhinaria ... ...R. coniuncta sp. n.

– Segment III three times as long as wide, with ca. 17 rows of rhinaria; M with 3 branches ...R. ennearticulata sp. n.

Rasnitsynaphis ennearticulatasp. n.

urn:lsid:zoobank.org:act:9040D3E2-3EFE-474D-889A-2408FD52A5BC http://species-id.net/wiki/Rasnitsynaphis_ennearticulata

Fig. 1

Material. Holotype: PIN 3064/2109(2211); Baissa, Transbaikalia; Zaza Formation, bed 31.

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Diagnosis. Antennae rather long; segment III three times as long as wide; seg-ments IV–VIII of about the same length, rectangular, longer than wide. Media with three branches.

Description. Length of the body 2.1 (Fig. 1c). Width of head 0.43 (Fig. 1a). Lat-eral sutures join in the middle of epicranium in the four fifth of the head length. On the dorsal side of head capsule there are three diagonal strips, running from the middle part of epicranium to the frontolateral edge of head. The distance between ocelli (situ-ated on the back of head) 0.27. Length of the apical segment of rostrum 0.18 (Fig 1e). Antennae 0.93 long, ca. 0.8 of thorax width (Figs 1b, d). Length of antennal segments: I 0.06; II 0.08; III 0.23; each of IV–VII 0.09; VIII 0.08; IX 0.07. Antennal segment III with about 17 rows of rhinaria, with at most 8 rhinaria arranged in one row. Seg-ments IV–VIII at most with 7 rows of rhinaria. Tibia of fore legs 0.75 long, middle tibiae 0.83 to 0.86. Mesothoracic sternite 0.93 wide, 0.53 long. Fore wings about 3.8 long. The distance from the base of the wing to the end of pterostigma 2.8. Distance

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between bases of cubital veins CuA1 & CuA2 0.14. The length of M1+2 more or less equals the length of the common stem of M. The posterior part of abdomen strongly sclerotized (Fig. 1f ).

Rasnitsynaphis coniunctasp. n.

urn:lsid:zoobank.org:act:197A9263-DFAA-4A61-9774-822FE7D3585D http://species-id.net/wiki/Rasnitsynaphis_coniuncta

Fig. 2

Material. Holotype: PIN 3064/2209; Baissa, Transbaikalia; Zaza Formation, bed 31.

Etymology. From the Latin term coniunctus for “joined” in reference to the joined rows of rhinaria.

Diagnosis. Antenna rather long; segment III four times as long as wide; segments IV–VIII of about the same length, rectangular, longer than wide.

Description. Length of the body about 2.4 (Fig. 2b). Head with epicranial suture. Antennae 0.88 long, about 2/3 of thorax height (Figs 2a, c). Length of antennal segments:

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II 0.12; III 0.24; IV 0.09; V 0.08; each of VI–VII 0.09; VIII 0.08; IX 0.07 to 0.08. Anten-nal segment III with 11 rows of rhinaria, with at most 7 rhinaria arranged in one row. Seg-ments IV–VIII at most with 6 rows of rhinaria. Femur of fore legs 0.74 long, tibia 1.06. Middle tibia 1.14 long. Hind femur 0.87 long, tibia 1.34. The second segment of hind leg tarsus 0.24 (Fig. 2d). The distance between bases of cubital veins CuA1 & CuA2 0.13.

Rasnitsynaphis quadrata sp. n.

urn:lsid:zoobank.org:act:7434FB55-DE6B-4C54-9086-F2E62111405D http://species-id.net/wiki/Rasnitsynaphis_quadrata

Fig. 3

Material. Holotype: 3064/2279; Baissa, Transbaikalia; Zaza Formation, bed 31.

Etymology. From the Latin term quadratus for “square” in reference to the square shape of antennal segments IV–VII.

Diagnosis. Antennae quite short; segment III two times as long as wide; segments IV–VII of the same length, square, as long as wide. Media with two branches.

Description. Length of the body 2.0 (Fig. 3b). Length of head 0.28. Head with lateral sutures. Length of the apical segment of rostrum 0.14 (Fig. 3c). Antennae 0.71

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long, about 1/2 of thorax height (Fig. 3a, b). Length of antennal segments: I 0.06; II 0.07; III 0.16; each of IV–IX 0.06. Antennal segment III with about 9 rows of rhi-naria, with at most 8 rhinaria arranged in one row. Segments IV–VIII at most with 4 rows of rhinaria. Femur of middle legs 0.54 long, tibia 0.73. Hind femur 0.57 long. Mesothoracic sternite 0.49 long. The distance from the base of the wing to the end of pterostigma 2.7. The distance between bases of cubital veins CuA1 & CuA2 0.11. The posterior part of abdomen weakly sclerotized.

Discussion

The family Rasnitsynaphididae fam. n. on the one hand possesses primitive features of Jurassic Sinojuraphididae Huang & Nel, 2008 and Genaphididae Handlirsch, 1907, but on the other hand the features typical for Early Cretaceous Oviparosiphidae and Ellinaphididae, and also certain features of recent Aphididae and Drepanosiphidae (Heie and Wegierek 2009).

The body morphology and wing venation of the new family are typical for Lower Cretaceous aphids. The 9-segmented antennae recorded in Rasnitsynaphididae is the plesiomorphic feature and proves the presence of forms intermediate between Mid-dle Jurassic Sinojuraphididae with 12-segmented antennae (Huang & Nel 2008) and Mesozoic and modern aphids with 7-, 6- or 5-segmented antennae. In the general structure of antenna, which is relatively short and massive, it resembles many repre-sentatives of Oviparosiphidae. Due to the arrangement of numerous small, ellipsoidal rhinaria in transverse rows, Rasnitsynaphididae is similar to Ellinaphididae and Juro-callis Shaposhnikov, 1979, however the length ratio of flagellum segments is different. In the shape of pterostigma and place of Rs separation Rasnitsynaphis is similar to the species of Oviparosiphum Shaposhnikov & Wegierek, 1989. In the structure of CuA and M veins Rasnitsynaphis resembles Bajsaphis Shaposhnikov, 1985, Acan-thotrichaphis Shaposhnikov & Wegierek, 1989, Vitimaphis Shaposhnikov & Wegierek, 1989, and other genera of the family Oviparosiphidae (Zhang et al. 1989). In the course of the M vein Rasnitsynaphis ennearticulata sp. n. is similar also to Penaphis Lin, 1980 (Jarzembowski 1989, Lin 1995) and some species of the families Aphididae and Drepanosiphidae (Shaposhnikov 1980).

Having so many features in common with the family Oviparosiphidae, the new family differs from it by the 9-segmented antennae and lack of siphunculi.

Acknowledgements

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References

Becker-Migdisova EE (1966) Aphid Aphis valdensis Brodie (Homoptera, Aphidinea) from the Upper Jurassic deposits of England (a revision of type). Entomologicheskoe Obozrenie 45: 579–583 [in Russian]

Heie OE, Wegierek P (2009) Diagnoses of the higher taxa of Aphidomorpha (Hemiptera: Ster-norrhyncha). Redia 92: 261–269.

Huang D, Nel A (2008) A new Middle Jurassic aphid family (Insecta: Hemiptera: Sternor-rhyncha: Sinojuraphididae fam. nov.) from inner Mongolia, China. Palaeontology 51: 715–719. doi: 10.1111/j.1475-4983.2008.00773.x

Jarzembowski EA (1989) A fossil aphid from the Early Cretaceous of southern England. Creta-ceous Research 10: 239–248. doi: 10.1016/0195-6671(89)90020-7

Lin QB (1995) On Penaphis Lin, 1980 of Cretaceous (Callaphididae, Homoptera) and its co-evolutionary relationships. Acta Palaeontologica Sinica 34: 194–204 [In Chinese, English summary]

Kania I, Wegierek P (2008) Palaeoaphididae (Hemiptera, Sternorrhyncha) from Lower Cre-taceous Baissa deposits. Morphology and classification. Instytut Systematyki i Ewolucji Zwierząt, Polska Akademia Nauk, Kraków, 135 pp.

Rasnitsyn AP (2002) Special features of the study of fossil insects. In: Rasnitsyn AP, Quicke DLJ (Eds) History of Insects. Kluwer Academic Publishers, Dordrecht, 8–12. doi: 10.1007/0-306-47577-4

Shaposhnikov GCh (1979) Late Jurassic and Early Cretaceous aphids. Paleontological Journal 1979(4): 66–78 [in Russian]

ShaposhnikovGCh (1980) Evolution of morphological structures in aphids (Homoptera, Aphi-dinea) and habits of the recent and Mesozoic representatives of the group. Entomologicheskoe Obozrenie 59: 39–59 [in Russian; English translation: Entomological Review 59: 29–48] ShaposhnikovGCh (1985) The main features of the evolution of aphids. In: Evolution and

Biosystematics of Aphids. Ossolineum, Wrocław, 19–99.

Shaposhnikov GCh, Wegierek P (1989) New aphids of the late Mesozoic (Oviparosiphidae, Homoptera). Paleontologicheski Zhurnal, 1989(3): 42–50 [in Russian]

Wegierek P (1989) New species of Mesozoic aphids (Shaposhnikovidae, Homoptera). Paleon-tologicheski Zhurnal, 1989(4): 43–51 [in Russian]

Węgierek P (1991) The aphid family Genaphididae (Homoptera, Aphidina) from the Upper Mesozoic of Mongolia. Polskie Pismo Entomologiczne, 68: 337–348.

Zhang JF, Zhang S, Hou F, Ma G (1989) Late Jurassic aphids (Homoptera, Insecta) from Shan-dong Province, China. Geology of ShanShan-dong, 5: 28–46 [in Chinese, English summary] Zherikhin VV, Mostovski MB, Vrsansky P, Blagoderov VA, Lukashevich ED (1999) The unique

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